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Content:
Chapter 1 Chairman's creation (page 1): William Mordue
Chapter 2 advent: The hyperlinks among ‘Wet’ and ‘Dry’ body structure (pages 2–6): David S. Saunders
Chapter three team spirit and variety in Insect Photoperiodism (pages 7–25): Sinzo Masaki
Chapter four The Circadian part in Photoperiodic Induction (pages 26–47): C. S. Pittendrigh, J. Elliott and T. Takamura
Chapter five Photoperiod Reception in Spider Mites: Photoreceptor, Clock and Counter (pages 48–64): A. Veerman and M. Vaz Nunes
Chapter 6 Long?Night Summation and Programming of Pupal Diapause within the Flesh?Fly, Sarcophaga argyrostoma (pages 65–96): David S. Saunders and Helen Bradley
Chapter 7 Genetic research of Geographical version in Photoperiodic Diapause and Pupal Eclosion Rhythm in Drosophila littoralis (pages 97–114): Pekka Lankinen and Jaakko Lumme
Chapter eight Neuronal association of a Circadian Clock within the Cockroach Leucophaea maderae (pages 115–135): Terry L. Page
Chapter nine Circadian?Clock regulate of Hormone Secretion in Samia Cynthia ricini (pages 136–149): Hironori Ishizaki, Akira Mizoguchi and Mariko Fujishita
Chapter 10 Circadian keep watch over of Haemolymph Ecdysteroid Titres and the Ecdysis Rhythm in Rhodnius prolixus (pages 150–169): C. G. H. metal and E. J. Ampleford
Chapter eleven Photoperiodic rules of Prothoracicotropic Hormone free up in overdue Larval, Prepupal and Pupal levels of Sarcophaga bullata (pages 170–188): Brian Roberts
Chapter 12 Reproductive Endocrinology and Photoperiodism in a Terrestrial Slug (pages 189–203): P. G. Sokolove, E. J. McCrone, J. van Minnen and W. C. Duncan
Chapter thirteen Photoperiodicity, Rhythmicity and Endocrinology of replica within the Snail Lymnaea stagnalis (pages 204–220): J. Joosse
Chapter 14 Physiological elements of the 2 Oscillators That keep watch over the Timing of Eclosion in Moths (pages 221–239): James W. Truman
Chapter 15 A hormonal foundation for the Photoperiodic keep an eye on of Polymorphism in Aphids (pages 240–258): Jim Hardie
Chapter sixteen Environmental indications, the Neuroendocrine method, and the rules of Larval Diapause within the Southwestern Corn Borer, Diatraea grandiosella (pages 259–275): G. Michael Chippendale

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Extra resources for Ciba Foundation Symposium 104 - Photoperiodic Regulation of Insect and Molluscan Hormones

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Entomol Exp Appl 14:212-222 Ireland RC, Berger EM, Sirotkin K, Yund MA, Osterbur D, Fristrom J 1982 Ecdysterone induces the transcription of four heat shock genes in Drosophilu S3 cells and imaginal discs. Dev Biol 93:498-507 Jones MDR, Reiter P 1975 Entrainment of pupation and adult activity rhythms during development in the mosquito Anopheles gumbiue. Nature (Lond) 254:242-244 Kikukawa S 1983 Geographical adaptations and seasonal time measurement of the southwestern corn borer, Diatrueu grundiosellu.

Miyake, southern; Hokkaido, northern. Left: 15min, 50 lux pulses. Hokkaido has a Type-1 (weak resetting) phase-response curve; Miyake has a Type-0 (strong resetting) curve. Right: 60 min, 50 lux pulses. Both races now show Type-0 phase-response curves. In both panels there is a clear phase-difference between the races: the Hokkaido phase-response curve lies to the left of Miyake-it is closer to the last-seen photoperiod. The strains differ in their ‘subjective light intensities’. Abscissae scales are in hours.

The mere existence of circadian surfaces, let alone their detail, also seems difficult to explain in terms of external coincidence. The multi-oscillatornature of circadian organization: ‘internal Coincidence’ models of photoperiodic induction A quite distinct type of model for the photoperiodic time-measurement was introduced independently by Pittendrigh (1960,1972,1981a) and Tyshchenko (1966) and is based on increasingly clear evidence that circadian systems comprise many oscillations whose mutual phase-relations could well be altered by a change in photoperiod.

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